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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 270190생성일: 2026년 10월 25일

Ethyl cyanoacetate → 3-(4-Ethylphenyl)-2-cyano-but-2-enoic acid ethyl ester

https://huagongshe.com/reaction/270190

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl cyanoacetateHCID 7764—
반응물4'-EthylacetophenoneHCID 13642—
반응물Ammonium AcetateHCID 517165—
용매Acetic AcidHCID 176—
용매BenzeneHCID 241—
용매Ethyl AcetateHCID 8857—
생성물3-(4-Ethylphenyl)-2-cyano-but-2-enoic acid ethyl esterHCID 4465094—

반응 단계

A mixture of 4′-ethylacetophenone (50 mmol), ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL), ammonium acetate (400 mg), and benzene (50 mL) is heated to reflux in a Dean-Stark apparatus. After approximately 10 hours, additional ethyl cyanoacetate (50 mmol), acetic acid (1.14 mL), and ammonium acetate (400 mg) are added. After an additional 10 hours, the reaction is cooled to room temperature, diluted with ethyl acetate (30 mL), washed with water (240 mL), brine (40 mL), and dried (Na2SO4). After filtering, the extract is concentrated in vacuo and the desired product, as a mixture of E and Z-isomers, is isolated by column chromatography on silica gel, eluting with 5% ethyl acetate in petroleum ether.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07449490B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-98bcddf5215f4ed68c4e1cba9a2ae903
출처 메모uspto-grants-2008_11